Genome-wide studies of von Willebrand Factor Propeptide Identify Loci Contributing to Variation in Propeptide Levels and von Willebrand Factor Clearance

BACKGROUND: Previous studies identified common variants at the ABO and VWF loci and unknown variants in a chromosome 2q12 linkage interval that contributed to the variation of plasma von Willebrand factor levels (VWF). While the association with ABO haplotypes can be explained by differential VWF cl...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:J Thromb Haemost
Auteurs principaux: Ozel, A.B., McGee, B., Siemieniak, D., Jacobi, P.M., Haberichter, S.L., Brody, L.C., Mills, J.L., Molloy, A.M., Ginsburg, D., Li, J.Z., Desch, K.C.
Format: Artigo
Langue:Inglês
Publié: 2016
Sujets:
Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5035595/
https://ncbi.nlm.nih.gov/pubmed/27359253
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jth.13401
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires